Juna Sathian

Dr. Juna Sathian

Department of Mathematics, Physics and Electrical Engineering, Northumbria University, Newcastle upon Tyne, UK

Research Focus & Metrics

Academic Career Length

16Years (2011-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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22 March 2018 in Nature
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Journal Article
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JBJonathan D. Breeze
Jonathan D. Breeze
ESEnrico Salvadori
Enrico Salvadori
Juna SathianJuna Sathian
Juna Sathian
NANeil McN. Alford
Neil McN. Alford
CKChristopher W. M. Kay
Christopher W. M. Kay

20 February 2015 in Nature Communications
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Journal Article
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JBJonathan Breeze
Jonathan Breeze
KTKe-Jie Tan
Ke-Jie Tan
BRBenjamin Richards
Benjamin Richards
Juna SathianJuna Sathian
Juna Sathian
MOMark Oxborrow
Mark Oxborrow
NANeil McN Alford
Neil McN Alford
Recently, the world’s first room-temperature maser was demonstrated. The maser consisted of a sapphire ring housing a crystal of pentacene-doped p-terphenyl, pumped by a pulsed rhodamine-dye laser. Stimulated emission of microwaves was aided by the high quality factor and small magnetic mode volume of the maser cavity yet the peak optical pumping power was 1.4 kW. Here we report dramatic miniaturization and 2 orders of magnitude reduction in optical pumping power for a room-temperature maser by coupling a strontium titanate resonator with the spin-polarized population inversion provided by triplet states in an optically excited pentacene-doped p-terphenyl crystal. We observe maser emission in a thimble-sized resonator using a xenon flash lamp as an optical pump source with peak optical power of 70 W. This is a significant step towards the goal of continuous maser operation.

28 September 2017 in npj Quantum Information
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Journal Article
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JBJonathan D. Breeze
Jonathan D. Breeze
ESEnrico Salvadori
Enrico Salvadori
Juna SathianJuna Sathian
Juna Sathian
NANeil McN. Alford
Neil McN. Alford
CKChristopher W. M. Kay
Christopher W. M. Kay
The strong coupling regime is essential for efficient transfer of excitations between states in different quantum systems on timescales shorter than their lifetimes. The coupling of single spins to microwave photons is very weak but can be enhanced by increasing the local density of states by reducing the magnetic mode volume of the cavity. In practice, it is difficult to achieve both small cavity mode volume and low cavity decay rate, so superconducting metals are often employed at cryogenic temperatures. For an ensembles of N spins, the spin–photon coupling can be enhanced by $$\sqrt N$$ N through collective spin excitations known as Dicke states. For sufficiently large N the collective spin–photon coupling can exceed both the spin decoherence and cavity decay rates, making the strong-coupling regime accessible. Here we demonstrate strong coupling and cavity quantum electrodynamics in a solid-state system at room-temperature. We generate an inverted spin-ensemble with N ~ 1015 by photo-exciting pentacene molecules into spin-triplet states with spin dephasing time $$T_2^*\sim 3$$ T 2 * ~ 3 μs. When coupled to a 1.45 GHz TE01δ mode supported by a high Purcell factor strontium titanate dielectric cavity ( $$V_{\mathrm{m}}\sim 0.25$$ V m ~ 0.25 cm3, Q ~ 8,500), we observe Rabi oscillations in the microwave emission from collective Dicke states and a 1.8 MHz normal-mode splitting of the resultant collective spin–photon polariton. We also observe a cavity protection effect at the onset of the strong-coupling regime which decreases the polariton decay rate as the collective coupling increases.

23 August 2018 in Scientific Reports
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HQHeng Qin
Heng Qin
DWDanyang Wu
Danyang Wu
Juna SathianJuna Sathian
Juna Sathian
XXXiangyu Xie
Xiangyu Xie
MRMary Ryan
Mary Ryan
XFXie Fang
Xie Fang
The multiplexing capacity of conventional fluorescence materials are significantly limited by spectral overlap and background interference, mainly due to their short-lived fluorescence lifetimes. Here, we adopt a novel Gd3+ doping strategy in NaYF4 host materials, realized tuning of upconversion photoluminescence (UCPL) lifetimes at selective emissions. Time-correlated single-photon counting (TCSPC), was applied to measure the photoluminescence lifetimes accurately. We demonstrated the large dynamic range of lifetimes of upconversion nanoparticles with good upconversion quantum yields, mainly owing to the dominance of high efficient energy transfer upconversion mechanism. The exceptional tunable properties of upconversion materials allow great potential for them to be utilized in biotechnology and life sciences.

8 June 2017 in Optics Express
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Journal Article
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Juna SathianJuna Sathian
Juna Sathian
JBJonathan D. Breeze
Jonathan D. Breeze
BRBenjamin Richards
Benjamin Richards
NANeil McN. Alford
Neil McN. Alford
MOMark Oxborrow
Mark Oxborrow
A luminescent concentrator functioning as a bright source of yellow light is reported. It comprises a waveguide made of cerium-doped YAG crystal, in the form of a long-thin rectangular strip, surrounded by flowing air and optically pumped from both sides with blue light from arrays of high-efficiency InGaN LEDs. Phosphor-converted yellow light, generated within the strip, is guided to a glass taper that is butt-coupled to one of the strip’s end faces. Up to 20 W of optical power, centered on 575 nm with a linewidth of 76 nm, can be continuously radiated into air from the taper’s 1.67 mm × 1.67 mm square output aperture. The intensity of the outputted light is significantly greater than what any yellow (AlGaInP) LED can directly produce (either singly or arrayed), with only a modest increase in linewidth. Furthermore, the wall-plug efficiency of the source exceeds that of any yellow laser. The concept allows for further substantial increases in intensity, total output power and wall-plug efficiency through scaling-up and engineering refinements.

7 April 2016 in The Journal of Physical Chemistry C
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Closed access
SBStuart Arthur Bogatko
Stuart Arthur Bogatko
PHPeter D. Haynes
Peter D. Haynes
Juna SathianJuna Sathian
Juna Sathian
JWJessica Wade
Jessica Wade
JKJi-Seon Kim
Ji-Seon Kim
MOMark Oxborrow
Mark Oxborrow